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AI chat coach may spot complications after joint replacement surgery

NCT ID NCT07120191

Knowledge-focused Sponsor: Concentra AI, inc Source: ClinicalTrials.gov ↗

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Aug 31, 2026 · Last updated Sep 01, 2026 · Updated 1 time

Summary

This study tests a communication tool called MyConnect Post-Op, which uses AI-guided conversations to support patients after knee or hip replacement surgery. About 650 adults aged 22 to 80 who are scheduled for joint replacement will use the app on their smartphones. The researchers will collect conversation logs to see how well the tool guides recovery, identifies potential complications, and offers recommendations.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
MyConnect Post-Op, a post-operative communication software that uses AI-guided conversations to support recovery
What this could lead to
If the tool works well, it could help joint replacement patients recover more safely at home by catching complications early and offering clear guidance.
What could go wrong
This is a data collection study, not a test of effectiveness, so it may not prove the tool improves outcomes. The AI's advice might not always be accurate, and patients could still need in-person care.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

652 people

The number who actually took part.

Started

May 2025

Finished

Jul 2026

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

community sample from orthopedic practices

Ages

22 to 80 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: Orthopedic patients scheduled for elective joint arthroplasty (single or double knee, or single or double hip replacement surgery). Age 22-80 years. Owns a smart phone. Speaks and understands written and spoken English. Ability to give written informed consent. Exclusion Criteria: Known diagnosis of a psychiatric disorder. Known opioid dependence in the Investigator's opinion that may complicate participation. Participation in another clinical trial investigating a drug, medical device, or a medical procedure in the 30 days preceding trial inclusion and throughout the duration of the trial. Any condition that in the Investigator's opinion may complicate or preclude the subject from participating in this trial, such as physical impairment or noncooperation

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Total hip replacement Total knee replacement

Contacts and locations

Locations

  • Kansas Joint and Spine

    Wichita, Kansas, 67226, United States

  • Mercy Medical Center

    Baltimore, Maryland, 21202, United States

  • OrthoAZ

    Phoenix, Arizona, 85018, United States

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